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NCT05868668 · ClinicalTrials.gov registry record · NA
Efficacy of Low-intensity Shockwave vs Radial Wave for Treatment of Erectile Dysfunction and Pelvic Pain
A NA study of Erectile Dysfunction and Chronic Pelvic Pain Syndrome, sponsored by The Cleveland Clinic.
- Recruiting
- Registry status
- NA
- Development phase
- 186
- Enrollment target
- 1
- Study location
NCT05868668: Recruiting NA study of Erectile Dysfunction and Chronic Pelvic Pain Syndrome, sponsored by The Cleveland Clinic.
NCT05868668 is a NA study of Erectile Dysfunction and Chronic Pelvic Pain Syndrome that is actively recruiting participants, run by The Cleveland Clinic. The registered enrollment target is 186 participants, below the 226-participant average among 33 other Erectile Dysfunction trials with a reported enrollment target (18% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05868668, a NA study of Erectile Dysfunction and Chronic Pelvic Pain Syndrome, is actively recruiting participants, sponsored by The Cleveland Clinic.
- RECRUITING
- Registry status
- NA
- Development phase
- 186 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study to perform a randomized, sham controlled analysis of the effectiveness of both fSWT and rWT in the relief of erectile dysfunction and chronic pelvic pain syndrome.
Primary Outcome
To evaluate change/minimum clinically important difference (MCID) of International Index of Erectile Function score. Score varies according to baseline ED severity, generally requiring higher value for more severe symptoms.
Conditions Studied
Interventions
- DEVICE Focused shockwave
- DEVICE Radial wave
- DEVICE Sham treatment
Study Locations (1)
Ohio
- Cleveland Clinic Foundation - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 186 participants |
| Start Date | 2023-09-19 |
| Est. Completion | 2026-06 |
| Phase | NA |
What NCT05868668 shows while recruiting
NCT05868668 is an interventional study that assigns participants to a tested intervention. The registered 186 participants enrollment target is mid-sized for trials with a published cap, below the 226-participant average among 33 other Erectile Dysfunction trials with a reported enrollment target (18% lower).
The record links to 7 conditions, with Erectile Dysfunction appearing as the primary indexed condition, and to 3 interventions - of which Focused shockwave is the first listed.
NCT05868668 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT05868668 about?
NCT05868668 is a clinical study titled "Efficacy of Low-intensity Shockwave vs Radial Wave for Treatment of Erectile Dysfunction and Pelvic Pain". The purpose of this study to perform a randomized, sham controlled analysis of the effectiveness of both fSWT and rWT in the relief of erectile dysfunction and chronic pelvic pain syndrome.
What is the current status of trial NCT05868668?
This trial is currently recruiting. It is a NA study. The enrollment target is 186 participants. The study started on 2023-09-19. Estimated completion is 2026-06.
What conditions does trial NCT05868668 study?
This clinical trial studies the following conditions: Erectile Dysfunction, Chronic Pelvic Pain Syndrome, Erectile Dysfunction Following Radical Prostatectomy, Chronic Prostatitis, Erectile Dysfunction Due to Arterial Insufficiency.
What interventions are being tested in trial NCT05868668?
The interventions under investigation include: Focused shockwave (DEVICE), Radial wave (DEVICE), Sham treatment (DEVICE).
Who is sponsoring clinical trial NCT05868668?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05868668 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Erectile Dysfunction
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05868668's enrollment target sits among peer trials
186 12th of 33 higher than 22 of 33 other Erectile Dysfunction trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Erectile Dysfunction trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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